RHAMM marks proliferative subpopulation of human colorectal cancer stem cells

Author:

Nakano Michitaka12ORCID,Taguchi Ryosuke1,Kikushige Yoshikane1,Isobe Taichi13ORCID,Miyawaki Kohta14ORCID,Mizuno Shinichi5,Tsuruta Nobuhiro1,Hanamura Fumiyasu1,Yamaguchi Kyoko1,Yamauchi Takuji1,Ariyama Hiroshi1ORCID,Kusaba Hitoshi1,Nakamura Masafumi6,Maeda Takahiro4,Kuo Calvin J.2,Baba Eishi7ORCID,Akashi Koichi1

Affiliation:

1. Department of Medicine and Biosystemic Science, Graduate School of Medical Sciences Kyushu University Fukuoka Japan

2. Department of Medicine, Division of Hematology Stanford University School of Medicine Stanford California USA

3. Institute for Stem Cell Biology and Regenerative Medicine Stanford University Stanford California USA

4. Division of Precision Medicine Kyushu University Hospital Fukuoka Japan

5. Department of Health Sciences, Faculty of Medical Sciences Kyushu University Fukuoka Japan

6. Department of Surgery and Oncology, Graduate School of Medical Sciences Kyushu University Fukuoka Japan

7. Department of Oncology and Social Medicine, Graduate School of Medical Sciences Kyushu University Fukuoka Japan

Abstract

AbstractThe cancer stem cell (CSC) theory features typically rare self‐renewing subpopulations that reconstitute the heterogeneous tumor. Identification of molecules that characterize the features of CSCs is a key imperative for further understanding tumor heterogeneity and for the development of novel therapeutic strategies. However, the use of conventional markers of CSCs is still insufficient for the isolation of bona fide CSCs. We investigated organoids that are miniature forms of tumor tissues by reconstructing cellular diversity to identify specific markers to characterize CSCs in heterogeneous tumors. Here, we report that the receptor for hyaluronan‐mediated motility (RHAMM) expresses in a subpopulation of CD44+ conventional human colorectal CSC fraction. Single‐cell transcriptomics of organoids highlighted RHAMM‐positive proliferative cells that revealed distinct characteristics among the various cell types. Prospectively isolated RHAMM+CD44+ cells from the human colorectal cancer tissues showed highly proliferative characteristics with a self‐renewal ability in comparison with the other cancer cells. Furthermore, inhibition of RHAMM strongly suppressed organoid formation in vitro and inhibited tumor growth in vivo. Our findings suggest that RHAMM is a potential therapeutic target because it is a specific marker of the proliferative subpopulation within the conventional CSC fraction.

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Shinnihon Foundation of Advanced Medical Treatment Research

Publisher

Wiley

Subject

Cancer Research,Oncology,General Medicine

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